scholarly journals Localised childhood vulvar pemphigoid: a rare case study

2021 ◽  
Vol 13 (3) ◽  
pp. 283-286
Author(s):  
A.S. Peeters ◽  
N Dhont ◽  
H Stals
Keyword(s):  
Case Report ◽  
Young Patient ◽  
Bullous Pemphigoid ◽  
Rare Variant ◽  
Rare Case ◽  
Vulvar Pain ◽  
Topical Corticosteroids ◽  
Favourable Prognosis ◽  
Prompt Response

In this case report we present a young patient with localised childhood vulvar pemphigoid. It is a rare variant of bullous pemphigoid with mostly a favourable prognosis and prompt response to potent topical corticosteroids. She presented with relapsing vulvar pain and lesions. Our case enlightens the recognition of this unusual subtype and the importance of performing a cutaneous biopsy.

Pemphigoid Nodularis

2015 ◽  
Vol 19 (2) ◽  
pp. 153-155 ◽  
Author(s):  
Waleed Al-Salhi ◽  
Ru'aa Alharithy
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Effective Treatment ◽  
Bullous Pemphigoid ◽  
Clinical Features ◽  
Rare Variant ◽  
Early Recognition ◽  
Prurigo Nodularis ◽  
Clinical Variant ◽  
Pemphigoid Nodularis

Background Pemphigoid nodularis is a rare clinical variant of bullous pemphigoid characterized by overlapping clinical features of both prurigo nodularis lesions and bullous pemphigoid blisters. The condition appears to be more common in females and is often resistant to treatment. Objective To raise awareness of this rare variant of bullous pemphigoid. Methods Case report. Results and Conclusion Dermatologists should include this variant in differential diagnosis of prurigo nodularis because early recognition can lead to an effective treatment for the prurigo component.

scholarly journals A case study of Kimura due to grade 1 superficial burn: A rare case report

2020 ◽  
Vol 18 (4) ◽  
pp. 1-8
Author(s):  
marzieh haghbeen ◽  
farhang hoshmand ◽  
alireza abbasi ◽  
elham rafie ◽  
athar rasekh jahromi ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report

scholarly journals A Rare Case of Bertolotti's Syndrome in a Young Patient: A Case Report and Literature Review

Cureus ◽  
2020 ◽  
Author(s):  
Jasvindar Kumar ◽  
Sundas Ali ◽  
Nasrullah Zadran ◽  
Manjeet Singh ◽  
Zahoor Ahmed
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Young Patient ◽  
Rare Case

scholarly journals Axillary crystallizing galactocele masqueradingmalignancy:A rare case report andreview of literature

2021 ◽  
Vol 6 (3) ◽  
pp. 142-144
Author(s):  
Swati Raj ◽  
Abhishek Baunihiyal ◽  
Shalini Shah ◽  
Naveen Thapliyal
Keyword(s):  
Case Report ◽  
Rare Variant ◽  
Rare Case ◽  
Benign Lesion ◽  
Amorphous Material ◽  
Rare Case Report ◽  
Lactating Breast ◽  
Lipid Micelles

Galactocele are the most common benign lesion in lactating breast, whereas crystallizing galactocele are the rare variant. Axillary crystallizing galactocele are extremely rare to see , most commonly occur due to wrong breastfeeding technique. FNAC smear shows variety of crystals along with cysteine like crystals in a background of granular amorphous material or lipid micelles.

scholarly journals Bladder Chondrosarcoma in A Male: A Rare Case Report

2021 ◽  
Vol 57 (3) ◽  
pp. 256
Author(s):  
Muhammad Husni Tamrin ◽  
Wahjoe Djatisoesanto
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Sarcoma ◽  
Rare Variant ◽  
Rare Case ◽  
Bladder Tumor ◽  
Histopathological Examination ◽  
Low Grade ◽  
Lower Abdomen ◽  
Rare Case Report

Chondrosarcoma is a rare variant of bladder tumor and one of the rare types of soft tissue sarcoma. This case happened on a 36-year-old male who complained of lumps in his lower abdomen, accompanied by difficulties in passing urine and painful urination, without hematuria. We performed TURBT and histopathological examination showed low-grade chondrosarcoma. The patient was diagnosed with low-grade bladder chondrosarcoma. The patient was treated for chemotherapy and radiotherapy. However, after undergoing one cycle of chemotherapy, the patient refused to continue the therapy.

scholarly journals Juvenile Polyposis Syndrome in a Young Patient: A Rare Case Report

2018 ◽  
Vol 3 (2) ◽  
pp. 492-494
Author(s):  
Yamuna Agrawal ◽  
Rajan Shah ◽  
Brikh Raj Joshi ◽  
Vivek Kattel
Keyword(s):  
Case Report ◽  
Young Patient ◽  
Rare Case ◽  
Juvenile Polyposis ◽  
Juvenile Polyposis Syndrome ◽  
Polyposis Syndrome ◽  
Rare Syndrome ◽  
Rare Case Report ◽  
Malignant Condition

Juvenile polyposis syndrome prevalence is 1 in 16,000 to 1 in 100,000 which usually present at the age of 20 years. The tumor is likely to change into malignant condition in 20% of cases. Here we present this rare syndrome in a 16-year boy. BJHS 2018;3(2)6:492-494.

scholarly journals Unilateral Lichen Planus: A Rare Case Report

2018 ◽  
Vol 16 (1) ◽  
pp. 70-71
Author(s):  
Niharika Jha ◽  
Bimal Kanish ◽  
Anuradha Bhatia
Keyword(s):  
Case Report ◽  
Lichen Planus ◽  
Rare Variant ◽  
Rare Case ◽  
The Body ◽  
Lumbar Region ◽  
Volar Aspect ◽  
Rare Case Report ◽  
The Right

Lichen planus (LP) is a papulosquamous disorder characterized by violaceous, flat topped papules and plaques seen on the volar aspect of the wrists, lumbar region and around the ankles. It can have a varied presentation. Here we describe a rare variant of LP in a female who presented with unilateral eruptions of violaceous papules over the right side of the body.

scholarly journals A Rare Case Report on Thoracoomphalopagus

2016 ◽  
Vol 11 (1) ◽  
pp. 62-64
Author(s):  
Sabina Lamichhane ◽  
B Banerjee ◽  
S Subedi
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Rare Case ◽  
Pregnancy Termination ◽  
Conjoined Twins ◽  
Second Trimester ◽  
Mortality And Morbidity ◽  
Rare Case Report ◽  
Present Case Study

In the present case study we are reporting a case of thoracoomphalopagus conjoined twins. A 24 years old gravida two para 0+1 carrying thoracoomphalopagus conjoined twins was diagnosed by ultrasonography at early second trimester with single placenta attached posteriorly and low lying. The mortality and morbidity of conjoined twins are high so making the early diagnosis with ultrasonographic examination provides the parents a chance to elect for pregnancy termination.

Sign in / Sign up

Export Citation Format

Share Document